werdnig-hoffmann disease 是什么意思，中文意思 | 韦德尼希-霍夫曼病,又称“婴儿型脊髓性肌萎缩”英文怎么说医学英语中英文词汇翻译

Duchenne's Muscular Dystrophy and Spinal Muscular Atrophy

D Schlenzka - Non-Idiopathic Spine Deformities in Young Children, 2011 - Springer
... Type I: Acute infantile (Werdnig–Hoffmann) It becomes evident at birth or during the first
months of life by muscle weakness and impaired breathing. ... Type II: Chronic infantile
(Werdnig–Hoffmann) It starts at an age between 6 and 18 months. ...
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Detection of Spinal Muscular Atrophy Carriers in a Sample of the Brazilian Population

KC Bueno, SP Gouvea, AB Genari… - …, 2011 - content.karger.com
... Lancet 1980;i:919–922. 2. Czeizel A, Hamula J: A Hungarian study on Werdnig-Hoffmann disease.
J Med Genet 1989;26:761–763. ... 16. Pearn JH: The gene frequency of acute Werdnig-Hofmann
disease (SMA type I). A total population survey in Northeast England. ...
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[PDF] Anesthetic management of spinal muscle atrophy type II in a parturient

[PDF] from dovepress.comL Bollag, CD Kent, P Richebé… - Local and Regional …, 2011 - dovepress.com
... SMA type I, first described by the Austrian and German neurologist duo of Werdnig Page
2. ... SMA type II, intermediate SMA, or in older literature referred to as chronic
Werdnig-Hoffman disease is diagnosed in the first 6–24 months after birth. ...
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New insights into the pathogenesis of spinal muscular atrophy

Y Ito, N Shibata, K Saito, M Kobayashi… - Brain and Development, 2011 - Elsevier
... neurological disorder characterized by progressive loss of lower motor neurons (LMNs) in the
spinal cord and lower brain stem, associated with a resultant neurogenic muscular atrophy [1]
and [2]. SMA is subclassified into three clinical phenotypes: Werdnig-Hoffmann disease ...
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Spinal Muscular Atrophy: A Timely Review

SJ Kolb… - Archives of Neurology, 2011 - Am Med Assoc
... a PowerPoint slide]. Figure 1. Spinal muscular atrophy (SMA) timeline. Spinal
muscular atrophy was first reported by Werdnig in 1891 and then by others who
recognized variability of muscle weakness severity. A century later ...
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… use of ivabradine in patients with stable coronary artery disease presented with chronic bacterial/viral infectionDifferentiation of Fabry Disease and amyloidosis among …

…, J Krieg, F Straube, S Reif, E Hoffmann… - …, 2011 - Eur Heart Rhythm Assoc

… approach for broken lead extraction using recaptured lead venous entry accessAuriculo-ventricular conduction in Sinus Node Disease during different physiologic …

…, J Brachmann, D Andresen, E Hoffmann… - …, 2011 - Eur Heart Rhythm Assoc

… Outcome of Radio-frequency ablation for monomorphic sustained Ventricular tachycardia in patients with underlying heart disease without implantation of a …

…, J Krieg, F Straube, E Hoffmann… - …, 2011 - Eur Heart Rhythm Assoc

Apolipoprotein E genotypes, circulating C-reactive protein and angiographic coronary artery disease (The Ludwigshafen Risk and Cardiovascular Health Study)

TB Grammer, MM Hoffmann, W Renner, ME Kleber… - Atherosclerosis, 2011 - Elsevier
C-reactive protein (CRP) has been implicated in the development of atherosclerosis. The
genetic polymorphism of apolipoprotein (apo) E is associated with the concentration of CRP.
We analyzed the association between the apo E genotype, CRP and angiographic ...
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[HTML] Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits

[HTML] from plos.org…, AR Shuldiner, JL Butler, M Tomas, U Hoffmann… - PLoS genetics, 2011 - dx.plos.org
NAFLD is a spectrum of disease that ranges from steatosis to steatohepatitis (nonalcoholic steatohepatitis
or NASH: inflammation around the fat) to fibrosis/cirrhosis. Hepatic steatosis can be measured
non-invasively using computed tomography (CT) whereas NASH/fibrosis is assessed ...
Cited by 8 - Related articles - Cached - All 14 versions

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[PDF] Anesthetic management of spinal muscle atrophy type II in a parturient

[HTML] Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits